Gray baby syndrome

From WikiMD.org
Jump to navigation Jump to search

Gray baby syndrome

Gray baby syndrome (pronounced: /ɡreɪ ˈbeɪbi ˈsɪndroʊm/) is a rare but serious side effect that occurs in newborn infants (especially premature babies) due to the accumulation of the antibiotic chloramphenicol.

Etymology

The term "Gray baby syndrome" is derived from the characteristic grayish discoloration observed in affected infants. The syndrome was first described in the 1950s, shortly after the introduction of chloramphenicol.

Symptoms

The symptoms of Gray baby syndrome may include a grayish color to the skin, hypotension (low blood pressure), cyanosis (blue color to the skin due to lack of oxygen), abdominal distension, vomiting, diarrhea, respiratory distress, and lethargy. In severe cases, it can lead to cardiovascular collapse and death.

Causes

Gray baby syndrome is primarily caused by the administration of high doses of chloramphenicol, especially in premature infants or newborns with impaired liver function. The immature liver in these infants is unable to metabolize and excrete the drug, leading to its accumulation and subsequent toxic effects.

Treatment

The treatment for Gray baby syndrome involves immediate discontinuation of chloramphenicol and supportive care. In some cases, hemodialysis may be required to remove the drug from the body.

Prevention

To prevent Gray baby syndrome, it is important to use chloramphenicol judiciously, especially in newborns and premature infants. The drug should be used only when absolutely necessary and in the lowest effective dose.

See also

External links

Esculaap.svg

This WikiMD dictionary article is a stub. You can help make it a full article.


Languages: - East Asian 中文, 日本, 한국어, South Asian हिन्दी, Urdu, বাংলা, తెలుగు, தமிழ், ಕನ್ನಡ,
Southeast Asian Indonesian, Vietnamese, Thai, မြန်မာဘာသာ, European español, Deutsch, français, русский, português do Brasil, Italian, polski